Lista de obras - Riccardo Magistroni - Dominio Público Uruguay

ADPKD current management and ongoing trials

artículo científico publicado en 2019

Can tonsillectomy modify the innate and adaptive immunity pathways involved in IgA nephropathy?

artículo científico publicado en 2014

Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy.

artículo científico publicado en 2012

Comment on the paper: 'novel approach to estimate kidney and cyst volumes using mid-slice magnetic resonance images in polycystic kidney disease'

article

Comparison of Total Kidney Volume Quantification Methods in Autosomal Dominant Polycystic Disease for a Comprehensive Disease Assessment

artículo científico publicado en 2017

Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).

artículo científico publicado en 2016

Defective glycolysis and the use of 2-deoxy-D-glucose in polycystic kidney disease: from animal models to humans.

artículo científico publicado en 2017

Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens.

artículo científico publicado en 2011

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

artículo científico publicado en 2014

Evaluation of the Classification Accuracy of the Kidney Biopsy Direct Immunofluorescence through Convolutional Neural Networks

scientific article published on 16 September 2020

Genetic variation of DKK3 may modify renal disease severity in ADPKD.

artículo científico publicado en 2010

Genome-Wide Linkage Scan of a Large Family with IgA Nephropathy Localizes a Novel Susceptibility Locus to Chromosome 2q36

artículo científico publicado en 2007

Genome-wide association study identifies susceptibility loci for IgA nephropathy

artículo científico publicado en 2011

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease

artículo científico publicado en 2003

Hybrid dialysis: a promising strategy to reduce hospital access during the SARS-CoV-2 pandemic

artículo científico publicado en 2020

Identification and characterization of a new autoimmune protein in membranous nephropathy by immunoscreening of a renal cDNA library

artículo científico publicado en 2012

Influence of ACE I/D gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney disease: a meta-analysis

scientific article published on 25 August 2006

Interstitial fluid obtained from kidney biopsy as new source of renal biomarkers.

artículo científico publicado en 2011

Lipoprotein glomerulopathy associated with a mutation in apolipoprotein e

artículo científico publicado en 2013

Lipoprotein glomerulopathy treated with LDL-apheresis (Heparin-induced Extracorporeal Lipoprotein Precipitation system): a case report

artículo científico publicado en 2009

Monoclonal antibodies in nephrology: a delicate balance between curative potential, evidence of effectiveness, and toxicity

artículo científico publicado el 1 de mayo de 2012

New developments in the genetics, pathogenesis, and therapy of IgA nephropathy

artículo científico publicado en 2015

Precocious activation of genes of the renin-angiotensin system and the fibrogenic cascade in IgA glomerulonephritis.

artículo científico publicado en 2003

Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney disease

artículo científico publicado en 2005

Proteomic analysis of urine from proteinuric patients shows a proteolitic activity directed against albumin.

artículo científico publicado en 2009

Reliability of Total Renal Volume Computation in Polycystic Kidney Disease From Magnetic Resonance Imaging.

artículo científico publicado en 2015

Screening for cerebral aneurysms in the ADPKD population: mandatory or potentially harmful?

artículo científico publicado el 1 de noviembre de 2011

The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed condition

artículo científico publicado en 2018

Tolvaptan: Clinical Evidence for Slowing the Progression of Autosomal Dominant Polycystic Kidney Disease

artículo científico publicado en 2017

Tonsillectomy in a European Cohort of 1,147 Patients with IgA Nephropathy

article

Unified criteria for ultrasonographic diagnosis of ADPKD.

artículo científico publicado en 2008

Lista de obras de Riccardo Magistroni

ADPKD current management and ongoing trials

Can tonsillectomy modify the innate and adaptive immunity pathways involved in IgA nephropathy?

Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy.

Comment on the paper: 'novel approach to estimate kidney and cyst volumes using mid-slice magnetic resonance images in polycystic kidney disease'

Comparison of Total Kidney Volume Quantification Methods in Autosomal Dominant Polycystic Disease for a Comprehensive Disease Assessment

Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).

Defective glycolysis and the use of 2-deoxy-D-glucose in polycystic kidney disease: from animal models to humans.

Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens.

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Evaluation of the Classification Accuracy of the Kidney Biopsy Direct Immunofluorescence through Convolutional Neural Networks

Genetic variation of DKK3 may modify renal disease severity in ADPKD.

Genome-Wide Linkage Scan of a Large Family with IgA Nephropathy Localizes a Novel Susceptibility Locus to Chromosome 2q36

Genome-wide association study identifies susceptibility loci for IgA nephropathy

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease

Hybrid dialysis: a promising strategy to reduce hospital access during the SARS-CoV-2 pandemic

Identification and characterization of a new autoimmune protein in membranous nephropathy by immunoscreening of a renal cDNA library

Influence of ACE I/D gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney disease: a meta-analysis

Interstitial fluid obtained from kidney biopsy as new source of renal biomarkers.

Lipoprotein glomerulopathy associated with a mutation in apolipoprotein e

Lipoprotein glomerulopathy treated with LDL-apheresis (Heparin-induced Extracorporeal Lipoprotein Precipitation system): a case report

Monoclonal antibodies in nephrology: a delicate balance between curative potential, evidence of effectiveness, and toxicity

New developments in the genetics, pathogenesis, and therapy of IgA nephropathy

Precocious activation of genes of the renin-angiotensin system and the fibrogenic cascade in IgA glomerulonephritis.

Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney disease

Proteomic analysis of urine from proteinuric patients shows a proteolitic activity directed against albumin.

Reliability of Total Renal Volume Computation in Polycystic Kidney Disease From Magnetic Resonance Imaging.

Screening for cerebral aneurysms in the ADPKD population: mandatory or potentially harmful?

The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed condition

Tolvaptan: Clinical Evidence for Slowing the Progression of Autosomal Dominant Polycystic Kidney Disease

Tonsillectomy in a European Cohort of 1,147 Patients with IgA Nephropathy

Unified criteria for ultrasonographic diagnosis of ADPKD.

Urine proteome analysis may allow noninvasive differential diagnosis of diabetic nephropathy ⬇️

[Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease]

[Diagnosis in Polycystic Kidney Disease]

[Genetics and genetic counseling]